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miR-17~92 微 RNA 簇内的三级接触调节 microRNA miR-92a-1 的生物发生和 mRNA 靶向。

MicroRNA miR-92a-1 biogenesis and mRNA targeting is modulated by a tertiary contact within the miR-17~92 microRNA cluster.

机构信息

Department of Biochemistry, University of Alberta, Edmonton, Alberta T6G 2H7, Canada and Department of Oncology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.

出版信息

Nucleic Acids Res. 2014 Apr;42(8):5234-44. doi: 10.1093/nar/gku133. Epub 2014 Feb 11.

Abstract

While functional mature microRNAs (miRNAs) are small ∼22 base oligonucleotides that target specific mRNAs, miRNAs are initially expressed as long transcripts (pri-miRNAs) that undergo sequential processing to yield the mature miRNAs. We have previously reported that the pri-miR-17∼92 cluster adopts a compact globular folded structure that internalizes a 3' core domain resulting in reduced miRNA maturation and subsequent mRNA targeting. Using a site-specific photo-cross-linker we have identified a tertiary contact within the 3' core domain of the pri-miRNA between a non-miRNA stem-loop and the pre-miR-19b hairpin. This tertiary contact is involved in the formation of the compact globular fold of the cluster while its disruption enhances miR-92a expression and mRNA targeting. We propose that this tertiary contact serves as a molecular scaffold to restrict expression of the proposed antiangiogenic miR-92a, allowing for the overall pro-angiogenic effect of miR-17∼92 expression.

摘要

功能成熟的 microRNAs(miRNAs)是靶向特定 mRNAs 的小约 22 个碱基的寡核苷酸,但 miRNA 最初是作为长转录本(pri-miRNAs)表达的,这些长转录本经过连续加工生成成熟的 miRNAs。我们之前曾报道过,pri-miR-17∼92 簇采用紧凑的球形折叠结构,内部包含一个 3'核心结构域,导致 miRNA 成熟减少,并随后靶向 mRNA。我们使用一种位点特异性光交联剂,在 pri-miRNA 的 3'核心结构域内鉴定到非 miRNA 茎环和 pre-miR-19b 发夹之间的三级接触。这种三级接触参与簇的紧凑球形折叠的形成,而其破坏增强了 miR-92a 的表达和 mRNA 靶向。我们提出,这种三级接触充当分子支架,限制拟血管生成 miR-92a 的表达,从而允许 miR-17∼92 表达的整体促血管生成作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b45c/4005684/6a315c80fe6a/gku133f1p.jpg

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